Traumatic Brain Injury and Post Concussion Syndrome For traumatic brain injury (TBI) and post concussion syndrome (PCS).


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Old 11-03-2013, 12:11 AM #1
todayistomorrow todayistomorrow is offline
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todayistomorrow todayistomorrow is offline
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Default Amantadine experiences?

I know this drug is off label treatment for concussions but my Dr. seems to think this could help me a lot. My main symptom is fogginess. I just started a new job where I have to get up at 5am, so by the time Friday comes, I'm usually feeling miserable.

Would appreciate hearing users experience on this drug and dosage they take. Do you crash on it? If you stopped taking it, how was withdrawal? Side effects?
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Old 11-03-2013, 01:03 AM #2
Mark in Idaho Mark in Idaho is offline
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Mark in Idaho Mark in Idaho is offline
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Your doctor is right. It could help you a lot. But the term is COULD. It helps some and is worthless to others.

It is an anti-viral drug used for influenza A. It has helped some with Parkinson's.

Look up the side-effects and decide if it is worth it.
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Old 11-03-2013, 08:49 AM #3
Mokey Mokey is offline
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I have taken it a few times...most recently for 7 months....100 mg in the morning. When i stopped before (it can cause insomnia), i wen back to feelng so lethargic and a bit like a zombie.

I feel that it helps with energy, and my hyperacusis and auditory problems were not as bad.

I was prescribed 200 mg....but never got up there. I am happy with 100 mg.

The times i stopped, i tapered off over a two week period. I don't think there are withdrawal problems if you do that. (reported, of course!).

I recommend people try it...it has no side effects for me other than possible sleep issues....but i had them pre-amantadine!
Good luck!
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What happened: Legs pulled forward by a parent's hockey stick while resting at the side of the rink at a family skate....sent me straight back. I hit the back of my head (with helmet) on the ice, bounced a few times, unconscious for a few minutes. September 11, 2011. Off work since then…I work part-time at home when I can. It has been hell but slowly feeling better (when I am alone☺).

Current symptoms: Vision problems (but 20/20 in each eye alone!) – convergence insufficiency – horizontal and vertical (heterophoria), problems with tracking and saccades, peripheral vision problems, eyes see different colour tints; tinnitus 24/7 both ears; hyperacusis (noise filter gone!), labyrinthian (inner ear) concussion, vestibular dysfunction (dizzy, bedspins, need to look down when walking); partial loss of sense of smell; electric shocks through head when doing too much; headaches; emotional lability; memory blanks; difficulty concentrating. I still can’t go into busy, noisy places. Fatigue. Executive functioning was affected – multi-tasking, planning, motivation. Slight aphasia. Shooting pain up neck and limited mobility at neck. Otherwise lucky!

Current treatments: Vestibular therapy, Vision therapy, amantadine (100 mg a day), acupuncture and physiotherapy for neck, slow return to exercise, magnesium, resveratrol, omega 3 fish oils, vitamins D, B and multi. Optimism and perserverance.
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